LEUKOSEP – SOLX B ADDITIVE SOLUTION (Haemonetics Manufacturing Inc)


Welcome to the PulseAid listing for the LEUKOSEP – SOLX B ADDITIVE SOLUTION drug offered from Haemonetics Manufacturing Inc. This pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Haemonetics Manufacturing Inc
NON-PROPRIETARY NAME: SOLX B ADDITIVE SOLUTION
SUBSTANCE NAME: DEXTROSE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: INTRAVENOUS
DOSAGE FORM: SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2013-05-15
END MARKETING DATE: 0000-00-00


LEUKOSEP – SOLX B ADDITIVE SOLUTION HUMAN PRESCRIPTION DRUG Details:

Item DescriptionLEUKOSEP – SOLX B ADDITIVE SOLUTION from Haemonetics Manufacturing Inc
LABELER NAME: Haemonetics Manufacturing Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 1.78(g/30mL)
START MARKETING DATE: 2013-05-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 53157-301_795f1082-9ede-47cb-9a22-5092787ecbb3
PRODUCT NDC: 53157-301
APPLICATION NUMBER: NDA110059

Other DEXTROSE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
B. Braun Medical Inc.Dextrose
Haemonetics Manufacturing IncLeukotrap – CP2D Solution
Haemonetics Manufacturing Inc.Nutricel Additive Solution – CP2D